Cargando…
PRKCQ rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population
PURPOSE: The PRKCQ and REL genes are said to be associated with multiple autoimmune diseases. This study investigated the association between these genes and Vogt-Koyanagi-Harada (VKH) syndrome in Han Chinese. METHODS: A two-stage case−control study was performed on three single nucleotide polymorph...
Autores principales: | Xu, Lei, Zhao, Tingting, Yuan, Gangxiang, Hou, Shengping, Zeng, Wenxin, Chen, Feilan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925663/ https://www.ncbi.nlm.nih.gov/pubmed/31908401 |
Ejemplares similares
-
Association of a NOS3 gene polymorphism with Behçet’s disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese
por: Zhou, Yan, et al.
Publicado: (2016) -
Association of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet’s Disease in Han Chinese
por: Lu, Sha, et al.
Publicado: (2016) -
TNFAIP3 Gene Polymorphisms in a Chinese Han Population with Vogt–Koyanagi–Harada Syndrome
por: Li, Hong, et al.
Publicado: (2013) -
Genetic Variation in the REL Gene Increases Risk of Behcet’s Disease in a Chinese Han Population but That of PRKCQ Does Not
por: Chen, Feilan, et al.
Publicado: (2016) -
Interleukin-10 gene polymorphisms are associated with Behcet’s disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population
por: Hu, Jianmin, et al.
Publicado: (2015)